Canonical Allele Identifier: CA2324749777
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191644C= , CM000681.2:g.15191644C= GRCh38
NC_000019.9:g.15302455C= , CM000681.1:g.15302455C= GRCh37
NC_000019.8:g.15163455C= NCBI36
NG_009819.1:g.14338G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.816G= MANE Select ENSP00000263388.1:p.Thr272=
ENST00000263388.6:c.816G= ENSP00000263388.1:p.Thr272=
ENST00000601011.1:c.813G= ENSP00000473138.1:p.Thr271=
NM_000435.2:c.816G= NP_000426.2:p.Thr272=
XM_005259924.3:c.816G= XP_005259981.1:p.Thr272=
XM_005259924.4:c.816G= XP_005259981.1:p.Thr272=
NM_000435.3:c.816G= MANE Select NP_000426.2:p.Thr272=